Senior Statistical Programmer (Oncology)

Job Title: Senior Statistical Programmer (Oncology) Location: India Employment Type: Full-Time Experience Required: 8+ Years Overview We are seeking an experienced Senior Statistical Programmer (Oncology) to support end-to-end clinical programming activities across oncology studies. This role requires strong technical proficiency, the ability to work independently, and effective collaboration within cross-functional and global teams. Core Responsibilities Program, validate, and maintain clinical trial datasets and outputs using SAS and R. Lead and execute the full spectrum of statistical programming deliverables, including: Creation and review of SDTM and ADaM specifications Development of SDTM and ADaM datasets TLF (Tables, Listings, Figures) programming Preparation of Define.xml and reviewers guides Develop, enhance, and maintain macros to support study and project requirements. Work independently with minimal oversight, ensuring timely and high-quality deliverables. Demonstrate a strong sense of ownership and accountability for assigned tasks. Communicate proactively with internal teams, providing clear updates and technical guidance. Identify opportunities for process improvements and contribute suggestions to strengthen team efficiency. Proven experience working on oncology clinical trials, with a strong understanding of oncology-specific endpoints and data structures. Participate actively in programming meetings, cross-functional discussions, and knowledge-sharing sessions. Preferred Qualifications Prior experience working in global or geographically distributed teams. In-depth knowledge of CDISC standards and regulatory submission requirements. Experience supporting FDA and PMDA submissions. Ability to manage multiple studies simultaneously and prioritize tasks effectively. Strong documentation, planning, and organizational skills. Experience mentoring or providing technical oversight to junior programmers. Job Title: Senior Statistical Programmer (Oncology) Location: India Employment Type: Full-Time Experience Required: 8+ Years Overview We are seeking an experienced Senior Statistical Programmer (Oncology) to support end-to-end clinical programming activities across oncology studies. This role requires strong technical proficiency, the ability to work independently, and effective collaboration within cross-functional and global teams. Core Responsibilities Program, validate, and maintain clinical trial datasets and outputs using SAS and R. Lead and execute the full spectrum of statistical programming deliverables, including: Creation and review of SDTM and ADaM specifications Development of SDTM and ADaM datasets TLF (Tables, Listings, Figures) programming Preparation of Define.xml and reviewers guides Develop, enhance, and maintain macros to support study and project requirements. Work independently with minimal oversight, ensuring timely and high-quality deliverables. Demonstrate a strong sense of ownership and accountability for assigned tasks. Communicate proactively with internal teams, providing clear updates and technical guidance. Identify opportunities for process improvements and contribute suggestions to strengthen team efficiency. Proven experience working on oncology clinical trials, with a strong understanding of oncology-specific endpoints and data structures. Participate actively in programming meetings, cross-functional discussions, and knowledge-sharing sessions. Preferred Qualifications Prior experience working in global or geographically distributed teams. In-depth knowledge of CDISC standards and regulatory submission requirements. Experience supporting FDA and PMDA submissions. Ability to manage multiple studies simultaneously and prioritize tasks effectively. Strong documentation, planning, and organizational skills. Experience mentoring or providing technical oversight to junior programmers.